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Progressive pseudorheumatoid dysplasia: report of a family and review.

Progressive pseudorheumatoid dysplasia: report of a family and review.

http://www.wikidata.org/entity/Q33679107

about

WISP3, the gene responsible for the human skeletal disease progressive pseudorheumatoid dysplasia, is not essential for skeletal function in mice Normal growth and development in mice over-expressing the CCN family member WISP3 The Impact of Genetic Diseases on Jordanians: Strategies Towards Prevention Inflammatory arthritis in children with osteochondrodysplasias.The CCN family member Wisp3, mutant in progressive pseudorheumatoid dysplasia, modulates BMP and Wnt signaling The diagnostic challenge of progressive pseudorheumatoid dysplasia (PPRD): a review of clinical features, radiographic features, and WISP3 mutations in 63 affected individuals.A homozygous deletion of exon 1 in WISP3 causes progressive pseudorheumatoid dysplasia in two siblings.Spondyloepiphyseal dysplasia tarda with progressive arthropathy associated with subcapsular cataract.Progressive Pseudorheumatoid Dysplasia Misdiagnosed as Seronegative Juvenile Idiopathic Arthritis.Ischiopubic and odontoid synchondrosis in a boy with progressive pseudorheumatoid chondrodysplasia.Progressive Pseudorheumatoid Dysplasia or JIA?Delayed-onset of progressive pseudorheumatoid dysplasia in a Chinese adult with a novel compound WISP3 mutation: a case report.Boy with short stature and joint pains.

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P2860

Progressive pseudorheumatoid dysplasia: report of a family and review.

http://www.wikidata.org/entity/Q33679107

description

1997 nî lūn-bûn

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1997 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

1997 թվականի հուլիսին հրատարակված գիտական հոդված

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1997年の論文

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1997年論文

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1997年論文

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1997年論文

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1997年論文

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1997年論文

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1997年论文

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name

Progressive pseudorheumatoid dysplasia: report of a family and review.

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Progressive pseudorheumatoid dysplasia: report of a family and review.

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type

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Progressive pseudorheumatoid dysplasia: report of a family and review.

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Progressive pseudorheumatoid dysplasia: report of a family and review.

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Progressive pseudorheumatoid dysplasia: report of a family and review.

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Progressive pseudorheumatoid dysplasia: report of a family and review.

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P2093

Omari HZ

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Qubain HI

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el-Shanti HE

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P2860

Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus

Genetic mapping of a locus for multiple epiphyseal dysplasia (EDM2) to a region of chromosome 1 containing a type IX collagen gene

Spondyloepiphyseal dysplasia tarda with progressive arthropathy.

Spondyloepiphyseal dysplasia tarda with progressive arthropathy: a rare disorder frequently diagnosed among Arabs.

International classification of osteochondrodysplasias. International Working Group on Constitutional Diseases of Bone.

Clinical--molecular correlations in the skeletal dysplasias.

The type II collagenopathies: a spectrum of chondrodysplasias.

Progressive pseudorheumatoid chondrodysplasia simulating juvenile rheumatoid arthritis.

Spondyloepiphyseal dysplasia associated with progressive arthropathy. An unusual disorder mimicking juvenile rheumatoid arthritis.

Progressive pseudorheumatoid arthritis of childhood (PPAC) and normal adult height.

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